Philips Issues Software Correction for MCOT Devices, Ensures Continued Patient Safety Without Equipment Recall
Amsterdam, Netherlands – Philips, a global leader in health technology, has issued an advisory concerning a significant software configuration issue within its Mobile Cardiac Outpatient Telemetry (MCOT) devices. This notification comes after Philips took rapid action to identify and address the flaw following routine post-market surveillance. No devices are being recalled or removed from circulation, mitigating concerns about patient safety and equipment availability. Philips has directed customers to adhere to the guidelines set forth in …